Acidic solutions with common ions

In very highly concentrated acid solutions, the commonly used measurement of pH is not applicable. See also pH (Hydrogen Ion Concentration). Rather, the acidity must be related to the degree of transformation of a base with its conjugate acid. In the Hammett acidity function, developed by Hammett and Deyrup in 1932. 

Red chromium(VI) oxide, Cr03, is the acid anhydride of two acids chromic acid, H2CrO, and dichromic acid, H2Cr207. Neither acid has been isolated in pure form, although chromate and dichromate salts are common. CrOj reacts with H2O to produce strongly acidic solutions containing hydrogen ions and (predominantly) dichromate ions. 

The high sodium ion concentration results in facile crystallisation of the sodium salt. This process of salting out with common salt may be used for recrystallisation, but sodium benzenesulphonate (and salts of other acids of comparable molecular weight) is so very soluble in water that the solution must be almost saturated with sodium chloride and consequently the product is likely to be contaminated with it. In such a case a pure product may be obtained by crystallisation from, or Soxhlet extraction with, absolute alcohol the sul-phonate is slightly soluble but the inorganic salts are almost insoluble. Very small amounts of sulphones are formed as by-products, but since these are insoluble in water, they separate when the reaction mixture is poured into water ... 

In common with other hydroxy organic acids, tartaric acid complexes many metal ions. Formation constants for tartaric acid chelates with various metal ions are as follows Ca, 2.9 Cu, 3.2 Mg, 1.4 and Zn, 2.7 (68). In aqueous solution, tartaric acid can be mildly corrosive toward carbon steels, but under normal conditions it is noncorrosive to stainless steels (Table 9) (27). 

Iron hahdes react with haHde salts to afford anionic haHde complexes. Because kon(III) is a hard acid, the complexes that it forms are most stable with F and decrease ki both coordination number and stabiHty with heavier haHdes. No stable F complexes are known. [FeF (H20)] is the predominant kon fluoride species ki aqueous solution. The [FeF ] ion can be prepared ki fused salts. Whereas six-coordinate [FeCy is known, four-coordinate complexes are favored for chloride. Salts of tetrahedral [FeCfy] can be isolated if large cations such as tetraphenfyarsonium or tetra alkylammonium are used. [FeBrJ is known but is thermally unstable and disproportionates to kon(II) and bromine. Complex anions of kon(II) hahdes are less common. [FeCfy] has been obtained from FeCfy by reaction with alkaH metal chlorides ki the melt or with tetraethyl ammonium chloride ki deoxygenated ethanol. 

The dissociation of hypochlorous acid depends on the pH. The unionized acid is present in greater quantities in acid solution, although in strongly acid solution the reaction with water is reversed and chlorine is Hberated. In alkaline solutions the hypochlorite ion OCL is increasingly Hberated as the pH is increased. The pH is important because unionized hypochlorous acid is largely responsible for the antimicrobial action of chlorine in water. Chlorine compounds are therefore more active in the acid or neutral range. The hypochlorites most commonly employed are sodium hypochlorite [7681-52-9] or calcium hypochlorite [7778-54-3]. 

The EPA defines corrosivity in terms of pH (i.e., wastes with pH <2 or >2.5) or in terms of ability to corrode steel (SAE 20) at a rate of >6.35 mm (0.250 in.) per year at a temperature of 55 C (13°F). This discussion will address corrosivity as it applies to acids and caustics. Acids are compounds that yield H ions (actually HjO ions) when dissolved in water. Common industrial acids include acetic, nitric, hydrochloric, and sulfuric acids. The terms concentrated and dilute refer to the concentrations in solution. Mixing a concentrated acid with enough water will produce a dilute acid. For example, a bottle of concentrated HCl direct from the manufacturer is approximately 12 N in HCl, while a solution of HCl used in a titration may be only 0.5 N. The latter is a dilute acid solution. 

Determination of barium as sulphate Discussion. This method is most widely employed. The effect of various interfering ions (e.g. calcium, strontium, lead, nitrate, etc., which contaminate the precipitate) is dealt with in Section 11.72 The solubility of barium sulphate in cold water is about 2.5 mg L"1 it is, however, greater in hot water or in dilute hydrochloric or nitric acid, and less in solutions containing a common ion. 

Just as there are weak acids, there are also weak bases. A weak base does not readily accept protons from water molecules but does quantitatively accept protons from hydronium ions. Ammonia is the most common weak base. Ammonia exists predominantly as NH3 molecules in aqueous solution, but it undergoes quantitative proton transfer with hydronium ions to generate ammonium ions ... 

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